Reske S N
Eur Heart J. 1985 Aug;6 Suppl B:39-47. doi: 10.1093/eurheartj/6.suppl_b.39.
Metabolism of 15(p-123I-phenyl-) pentadecanoic acid (I-PPA) was investigated in Langendorff perfused rat hearts, fasted Wistar rats, pentobarbital-anaesthetized dogs and, in clinical studies, in patients with coronary artery disease. In murine experiments metabolism of I-PPA was compared quantitatively with 1-14 C-palmitic acid in double tracer studies. In these experiments I-PPA is taken up and metabolized very similarly to palmitic acid. Metabolic intervention studies showed identical directional changes of the rate of cardiac I-PPA and palmitic acid-oxidation during isoproterenol stimulated or lactate-suppressed cardiac lipolysis. Total heart uptake and turnover, as well as kinetics of labelled cardiac lipids, were found to be highly significantly related, when 14C-palmitic acid- and I-PPA-metabolism were analysed in vivo in an identical metabolic environment. In canine experiments initial uptake of I-PPA in the heart muscle is related to regional myocardial blood flow under control conditions and in ischaemia. Pacing induced hyperaemia is associated with an only moderate increase of I-PPA uptake, resulting in a threshold value at flow rates of about 150-200 ml min-1 (100 g-1) In clinical studies, myocardial infarcts can be accurately detected, localized and potentially quantitated. In significant coronary artery disease (greater than 75% diameter reduction), detection rates of 50-75% are found in studies performed at rest. Regional abnormalities of cardiac kinetics of I-PPA were found in about 60% of segments dependent on highly stenosed vessels (greater than 75% diameter reduction).(ABSTRACT TRUNCATED AT 250 WORDS)
在Langendorff灌注大鼠心脏、禁食的Wistar大鼠、戊巴比妥麻醉的犬以及在临床研究中,对患有冠状动脉疾病的患者体内,研究了15(对 - 123I - 苯基)十五烷酸(I - PPA)的代谢情况。在小鼠实验中,通过双示踪研究将I - PPA的代谢与1 - 14C - 棕榈酸进行了定量比较。在这些实验中,I - PPA的摄取和代谢与棕榈酸非常相似。代谢干预研究表明,在异丙肾上腺素刺激或乳酸抑制的心脏脂肪分解过程中,心脏I - PPA和棕榈酸氧化速率的方向变化相同。当在相同的代谢环境中对14C - 棕榈酸和I - PPA代谢进行体内分析时,发现心脏总摄取和周转以及标记心脏脂质的动力学高度显著相关。在犬实验中,心肌中I - PPA的初始摄取与对照条件下和缺血时的局部心肌血流量有关。起搏诱导的充血仅与I - PPA摄取的适度增加相关,在流速约为150 - 200 ml·min-1(100 g-1)时达到阈值。在临床研究中,可以准确检测、定位并可能定量心肌梗死。在严重冠状动脉疾病(直径减少大于75%)中,静息状态下的研究发现检测率为50 - 75%。在约60%依赖于高度狭窄血管(直径减少大于75%)的节段中发现了I - PPA心脏动力学的局部异常。(摘要截断于250字)